Lead, cGMP Peptide Manufacturing

CSBio Co.

Milpitas (CA)

On-site

USD 120,000 - 180,000

Full time

8 days ago
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Benefits offered by this job

401k
PTO
Medical, dental, and vision insurance
Holiday pay and paid time off
Disability insurance
Life insurance
Carpool / transportation assistance
Team building activities

Job summary

CSBio is seeking a Supervisor of cGMP Peptide Manufacturing at its Milpitas facility. You will lead production operations, oversee SPPS, purification, lyophilization, and packaging for clinical and commercial campaigns, reporting to the Head of Manufacturing.

This is a hands-on leadership role with responsibility for schedule, quality, and compliance. You will manage production staff, drive improvements, ensure 21 CFR 210/211 and ICH Q7 adherence, and support tech transfer and regulatory data

Qualifications

  • Bachelors degree in Chemistry, Biochemistry, Chemical Engineering or related discipline.
  • 3+ years of cGMP manufacturing experience in pharmaceutical, biopharmaceutical or peptide manufacturing.
  • Hands-on experience with SPPS, prep HPLC purification, and lyophilization.

Responsibilities

  • Lead and mentor manufacturing team; establish performance metrics and training.
  • Direct cGMP peptide production operations including SPPS, cleavage, purification, lyophilization, and packaging.
  • Own production scheduling and on-time delivery; allocate resources across programs.
  • Drive yield, throughput, and cost improvements using process capability data.

Skills

SPPS
cGMP manufacturing
Leadership
HPLC purification
Lyophilization
MES/eBR systems

Education

Bachelors in Chemistry/Biochemistry/Chemical Engineering or related

Tools

MES/eBR systems

Job description

CSBio is seeking a Supervisor of cGMP Peptide Manufacturing at its Milpitas facility. You will lead production operations, oversee SPPS, purification, lyophilization, and packaging for clinical and commercial campaigns, reporting to the Head of Manufacturing.

This is a hands-on leadership role with responsibility for schedule, quality, and compliance. You will manage production staff, drive improvements, ensure 21 CFR 210/211 and ICH Q7 adherence, and support tech transfer and regulatory data

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